TWI405572B - 新穎的胺基菸酸及異菸酸衍生物 - Google Patents

Info

Publication number

TWI405572B

TWI405572B TW096148215A TW96148215A TWI405572B TW I405572 B TWI405572 B TW I405572B TW 096148215 A TW096148215 A TW 096148215A TW 96148215 A TW96148215 A TW 96148215A TW I405572 B TWI405572 B TW I405572B

Authority

TW

Taiwan

Prior art keywords

ylamino

group

nicotinic acid

acid

compound

Prior art date

2006-12-22

Links

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• Global Dossier
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• KPIVDNYJNOPGBE-UHFFFAOYSA-N 2-aminonicotinic acid Chemical compound NC1=NC=CC=C1C(O)=O KPIVDNYJNOPGBE-UHFFFAOYSA-N 0.000 title 1
• TWBYWOBDOCUKOW-UHFFFAOYSA-N isonicotinic acid Chemical class OC(=O)C1=CC=NC=C1 TWBYWOBDOCUKOW-UHFFFAOYSA-N 0.000 title 1
• 150000001875 compounds Chemical class 0.000 claims abstract description 85
• 150000003839 salts Chemical class 0.000 claims abstract description 11
• 239000008194 pharmaceutical composition Substances 0.000 claims abstract description 6
• 150000001204 N-oxides Chemical class 0.000 claims abstract description 4
• PVNIIMVLHYAWGP-UHFFFAOYSA-N Niacin Chemical compound OC(=O)C1=CC=CN=C1 PVNIIMVLHYAWGP-UHFFFAOYSA-N 0.000 claims description 52
• -1 Nicotinate 2-(3-methyl-3'-(trifluoromethoxy)biphenyl-4-ylamino)nicotinic acid 2 -(3-chloro-3'-methoxybiphenyl-4-ylamino)nicotinic acid Chemical compound 0.000 claims description 46
• 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 45
• 125000005843 halogen group Chemical group 0.000 claims description 43
• 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 35
• 125000001424 substituent group Chemical group 0.000 claims description 35
• 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims description 32
• 235000001968 nicotinic acid Nutrition 0.000 claims description 29
• 239000011664 nicotinic acid Substances 0.000 claims description 29
• 201000010099 disease Diseases 0.000 claims description 27
• 125000001153 fluoro group Chemical group F* 0.000 claims description 25
• 239000003112 inhibitor Substances 0.000 claims description 25
• 229960003512 nicotinic acid Drugs 0.000 claims description 25
• 239000002253 acid Substances 0.000 claims description 24
• 108010052167 Dihydroorotate Dehydrogenase Proteins 0.000 claims description 23
• 102100032823 Dihydroorotate dehydrogenase (quinone), mitochondrial Human genes 0.000 claims description 23
• 229910052731 fluorine Inorganic materials 0.000 claims description 23
• 125000003545 alkoxy group Chemical group 0.000 claims description 21
• 238000011282 treatment Methods 0.000 claims description 20
• 125000004433 nitrogen atom Chemical group N* 0.000 claims description 15
• 206010039073 rheumatoid arthritis Diseases 0.000 claims description 14
• 201000001263 Psoriatic Arthritis Diseases 0.000 claims description 13
• 208000036824 Psoriatic arthropathy Diseases 0.000 claims description 13
• 125000000000 cycloalkoxy group Chemical group 0.000 claims description 13
• 230000005764 inhibitory process Effects 0.000 claims description 13
• 229910052757 nitrogen Inorganic materials 0.000 claims description 13
• 206010072579 Granulomatosis with polyangiitis Diseases 0.000 claims description 12
• 201000004681 Psoriasis Diseases 0.000 claims description 12
• 201000006417 multiple sclerosis Diseases 0.000 claims description 12
• 201000000596 systemic lupus erythematosus Diseases 0.000 claims description 12
• 239000003814 drug Substances 0.000 claims description 11
• 201000000306 sarcoidosis Diseases 0.000 claims description 11
• 206010002556 Ankylosing Spondylitis Diseases 0.000 claims description 10
• WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 10
• GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 10
• 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 10
• 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims description 9
• 229910052794 bromium Inorganic materials 0.000 claims description 9
• 239000001257 hydrogen Substances 0.000 claims description 9
• 229910052739 hydrogen Inorganic materials 0.000 claims description 9
• 150000001768 cations Chemical class 0.000 claims description 8
• 125000004429 atom Chemical group 0.000 claims description 7
• 229910052801 chlorine Inorganic materials 0.000 claims description 7
• 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims description 7
• 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 7
• 230000001575 pathological effect Effects 0.000 claims description 7
• 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 claims description 6
• 108010022394 Threonine synthase Proteins 0.000 claims description 6
• 102000004419 dihydrofolate reductase Human genes 0.000 claims description 6
• 239000003795 chemical substances by application Substances 0.000 claims description 5
• 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 5
• 239000002464 receptor antagonist Substances 0.000 claims description 5
• 229940044551 receptor antagonist Drugs 0.000 claims description 5
• 229960004641 rituximab Drugs 0.000 claims description 5
• HMLGSIZOMSVISS-ONJSNURVSA-N (7r)-7-[[(2z)-2-(2-amino-1,3-thiazol-4-yl)-2-(2,2-dimethylpropanoyloxymethoxyimino)acetyl]amino]-3-ethenyl-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid Chemical compound N([C@@H]1C(N2C(=C(C=C)CSC21)C(O)=O)=O)C(=O)\C(=N/OCOC(=O)C(C)(C)C)C1=CSC(N)=N1 HMLGSIZOMSVISS-ONJSNURVSA-N 0.000 claims description 4
• 125000004793 2,2,2-trifluoroethoxy group Chemical group FC(CO*)(F)F 0.000 claims description 4
• 102000051628 Interleukin-1 receptor antagonist Human genes 0.000 claims description 4
• 108700021006 Interleukin-1 receptor antagonist Proteins 0.000 claims description 4
• 229960004238 anakinra Drugs 0.000 claims description 4
• 229910052799 carbon Inorganic materials 0.000 claims description 4
• 125000001309 chloro group Chemical group Cl* 0.000 claims description 4
• BGISFYHWLSYDCI-UHFFFAOYSA-M lithium;pyridine-3-carboxylate Chemical compound [Li+].[O-]C(=O)C1=CC=CN=C1 BGISFYHWLSYDCI-UHFFFAOYSA-M 0.000 claims description 4
• UEJMTWHXKJKXEU-UHFFFAOYSA-N lithium;pyridine-4-carboxylic acid Chemical compound [Li].OC(=O)C1=CC=NC=C1 UEJMTWHXKJKXEU-UHFFFAOYSA-N 0.000 claims description 4
• 238000004519 manufacturing process Methods 0.000 claims description 4
• MZOFCQQQCNRIBI-VMXHOPILSA-N (3s)-4-[[(2s)-1-[[(2s)-1-[[(1s)-1-carboxy-2-hydroxyethyl]amino]-4-methyl-1-oxopentan-2-yl]amino]-5-(diaminomethylideneamino)-1-oxopentan-2-yl]amino]-3-[[2-[[(2s)-2,6-diaminohexanoyl]amino]acetyl]amino]-4-oxobutanoic acid Chemical compound OC[C@@H](C(O)=O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(O)=O)NC(=O)CNC(=O)[C@@H](N)CCCCN MZOFCQQQCNRIBI-VMXHOPILSA-N 0.000 claims description 3
• ZVCGCHFXVUBZIC-UHFFFAOYSA-N 2-[2,3,5,6-tetrafluoro-4-(3-methoxyphenyl)anilino]pyridine-3-carboxylic acid Chemical compound COC1=CC=CC(C=2C(=C(F)C(NC=3C(=CC=CN=3)C(O)=O)=C(F)C=2F)F)=C1 ZVCGCHFXVUBZIC-UHFFFAOYSA-N 0.000 claims description 3
• JBNWDYGOTHQHOZ-UHFFFAOYSA-N 2-[5-[4-[(4-fluorophenyl)methyl]piperidine-1-carbonyl]-6-methoxy-1-methylindol-3-yl]-n,n-dimethyl-2-oxoacetamide Chemical compound COC1=CC=2N(C)C=C(C(=O)C(=O)N(C)C)C=2C=C1C(=O)N(CC1)CCC1CC1=CC=C(F)C=C1 JBNWDYGOTHQHOZ-UHFFFAOYSA-N 0.000 claims description 3
• RQVKVJIRFKVPBF-VWLOTQADSA-N 2-[[(2s)-2-amino-3-phenylpropyl]amino]-3-methyl-5-naphthalen-2-yl-6-pyridin-4-ylpyrimidin-4-one Chemical compound C([C@H](N)CNC=1N(C(C(C=2C=C3C=CC=CC3=CC=2)=C(C=2C=CN=CC=2)N=1)=O)C)C1=CC=CC=C1 RQVKVJIRFKVPBF-VWLOTQADSA-N 0.000 claims description 3
• QSUSKMBNZQHHPA-UHFFFAOYSA-N 4-[4-(4-fluorophenyl)-1-(3-phenylpropyl)-5-pyridin-4-ylimidazol-2-yl]but-3-yn-1-ol Chemical compound C=1C=CC=CC=1CCCN1C(C#CCCO)=NC(C=2C=CC(F)=CC=2)=C1C1=CC=NC=C1 QSUSKMBNZQHHPA-UHFFFAOYSA-N 0.000 claims description 3
• IFGWYHGYNVGVRB-UHFFFAOYSA-N 5-(2,4-difluorophenoxy)-n-[2-(dimethylamino)ethyl]-1-(2-methylpropyl)indazole-6-carboxamide Chemical compound CN(C)CCNC(=O)C=1C=C2N(CC(C)C)N=CC2=CC=1OC1=CC=C(F)C=C1F IFGWYHGYNVGVRB-UHFFFAOYSA-N 0.000 claims description 3
• QZSUASFQOGKQPZ-UHFFFAOYSA-N 5-bromo-2-[2-fluoro-4-[3-(trifluoromethoxy)phenyl]anilino]pyridine-3-carboxylic acid Chemical compound OC(=O)C1=CC(Br)=CN=C1NC1=CC=C(C=2C=C(OC(F)(F)F)C=CC=2)C=C1F QZSUASFQOGKQPZ-UHFFFAOYSA-N 0.000 claims description 3
• 229940124292 CD20 monoclonal antibody Drugs 0.000 claims description 3
• 102000004631 Calcineurin Human genes 0.000 claims description 3
• 108010042955 Calcineurin Proteins 0.000 claims description 3
• 229930105110 Cyclosporin A Natural products 0.000 claims description 3
• PMATZTZNYRCHOR-CGLBZJNRSA-N Cyclosporin A Chemical compound CC[C@@H]1NC(=O)[C@H]([C@H](O)[C@H](C)C\C=C\C)N(C)C(=O)[C@H](C(C)C)N(C)C(=O)[C@H](CC(C)C)N(C)C(=O)[C@H](CC(C)C)N(C)C(=O)[C@@H](C)NC(=O)[C@H](C)NC(=O)[C@H](CC(C)C)N(C)C(=O)[C@H](C(C)C)NC(=O)[C@H](CC(C)C)N(C)C(=O)CN(C)C1=O PMATZTZNYRCHOR-CGLBZJNRSA-N 0.000 claims description 3
• 108010036949 Cyclosporine Proteins 0.000 claims description 3
• 108010008165 Etanercept Proteins 0.000 claims description 3
• 102000019223 Interleukin-1 receptor Human genes 0.000 claims description 3
• 108050006617 Interleukin-1 receptor Proteins 0.000 claims description 3
• UETNIIAIRMUTSM-UHFFFAOYSA-N Jacareubin Natural products CC1(C)OC2=CC3Oc4c(O)c(O)ccc4C(=O)C3C(=C2C=C1)O UETNIIAIRMUTSM-UHFFFAOYSA-N 0.000 claims description 3
• FBOZXECLQNJBKD-ZDUSSCGKSA-N L-methotrexate Chemical compound C=1N=C2N=C(N)N=C(N)C2=NC=1CN(C)C1=CC=C(C(=O)N[C@@H](CCC(O)=O)C(O)=O)C=C1 FBOZXECLQNJBKD-ZDUSSCGKSA-N 0.000 claims description 3
• 108010057466 NF-kappa B Proteins 0.000 claims description 3
• 239000012826 P38 inhibitor Substances 0.000 claims description 3
• 108700042805 TRU-015 Proteins 0.000 claims description 3
• QJJXYPPXXYFBGM-LFZNUXCKSA-N Tacrolimus Chemical compound C1C[C@@H](O)[C@H](OC)C[C@@H]1\C=C(/C)[C@@H]1[C@H](C)[C@@H](O)CC(=O)[C@H](CC=C)/C=C(C)/C[C@H](C)C[C@H](OC)[C@H]([C@H](C[C@H]2C)OC)O[C@@]2(O)C(=O)C(=O)N2CCCC[C@H]2C(=O)O1 QJJXYPPXXYFBGM-LFZNUXCKSA-N 0.000 claims description 3
• 108060008682 Tumor Necrosis Factor Proteins 0.000 claims description 3
• 102000000852 Tumor Necrosis Factor-alpha Human genes 0.000 claims description 3
• 230000004913 activation Effects 0.000 claims description 3
• 229960002964 adalimumab Drugs 0.000 claims description 3
• 239000005557 antagonist Substances 0.000 claims description 3
• 229960003115 certolizumab pegol Drugs 0.000 claims description 3
• 125000001995 cyclobutyl group Chemical group [H]C1([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims description 3
• 229960000403 etanercept Drugs 0.000 claims description 3
• 125000004785 fluoromethoxy group Chemical group [H]C([H])(F)O* 0.000 claims description 3
• 229960001743 golimumab Drugs 0.000 claims description 3
• 229960000598 infliximab Drugs 0.000 claims description 3
• 229960000485 methotrexate Drugs 0.000 claims description 3
• ICIJBYYMEBOTQP-UHFFFAOYSA-N n-[5-tert-butyl-3-(methanesulfonamido)-2-methoxyphenyl]-2-[4-(2-morpholin-4-ylethoxy)naphthalen-1-yl]-2-oxoacetamide;hydrochloride Chemical compound Cl.C1=C(C(C)(C)C)C=C(NS(C)(=O)=O)C(OC)=C1NC(=O)C(=O)C(C1=CC=CC=C11)=CC=C1OCCN1CCOCC1 ICIJBYYMEBOTQP-UHFFFAOYSA-N 0.000 claims description 3
• NCEXYHBECQHGNR-QZQOTICOSA-N sulfasalazine Chemical compound C1=C(O)C(C(=O)O)=CC(\N=N\C=2C=CC(=CC=2)S(=O)(=O)NC=2N=CC=CC=2)=C1 NCEXYHBECQHGNR-QZQOTICOSA-N 0.000 claims description 3
• 229960001940 sulfasalazine Drugs 0.000 claims description 3
• NCEXYHBECQHGNR-UHFFFAOYSA-N sulfasalazine Natural products C1=C(O)C(C(=O)O)=CC(N=NC=2C=CC(=CC=2)S(=O)(=O)NC=2N=CC=CC=2)=C1 NCEXYHBECQHGNR-UHFFFAOYSA-N 0.000 claims description 3
• QJJXYPPXXYFBGM-SHYZHZOCSA-N tacrolimus Natural products CO[C@H]1C[C@H](CC[C@@H]1O)C=C(C)[C@H]2OC(=O)[C@H]3CCCCN3C(=O)C(=O)[C@@]4(O)O[C@@H]([C@H](C[C@H]4C)OC)[C@@H](C[C@H](C)CC(=C[C@@H](CC=C)C(=O)C[C@H](O)[C@H]2C)C)OC QJJXYPPXXYFBGM-SHYZHZOCSA-N 0.000 claims description 3
• 229960001967 tacrolimus Drugs 0.000 claims description 3
• ZMELOYOKMZBMRB-DLBZAZTESA-N talmapimod Chemical compound C([C@@H](C)N(C[C@@H]1C)C(=O)C=2C(=CC=3N(C)C=C(C=3C=2)C(=O)C(=O)N(C)C)Cl)N1CC1=CC=C(F)C=C1 ZMELOYOKMZBMRB-DLBZAZTESA-N 0.000 claims description 3
• 229960005289 voclosporin Drugs 0.000 claims description 3
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• BICRTLVBTLFLRD-PTWUADNWSA-N voclosporin Chemical compound CC[C@@H]1NC(=O)[C@H]([C@H](O)[C@H](C)C\C=C\C=C)N(C)C(=O)[C@H](C(C)C)N(C)C(=O)[C@H](CC(C)C)N(C)C(=O)[C@H](CC(C)C)N(C)C(=O)[C@@H](C)NC(=O)[C@H](C)NC(=O)[C@H](CC(C)C)N(C)C(=O)[C@H](C(C)C)NC(=O)[C@H](CC(C)C)N(C)C(=O)CN(C)C1=O BICRTLVBTLFLRD-PTWUADNWSA-N 0.000 claims description 3
• 125000006273 (C1-C3) alkyl group Chemical group 0.000 claims description 2
• OMPATGZMNFWVOH-UHFFFAOYSA-N 2-[2,6-difluoro-4-(3-methoxyphenyl)anilino]pyridine-3-carboxylic acid Chemical compound COC1=CC=CC(C=2C=C(F)C(NC=3C(=CC=CN=3)C(O)=O)=C(F)C=2)=C1 OMPATGZMNFWVOH-UHFFFAOYSA-N 0.000 claims description 2
• ZJVWBRDJQSEWGP-UHFFFAOYSA-N 2-[2,6-difluoro-4-[3-(trifluoromethoxy)phenyl]anilino]pyridine-3-carboxylic acid Chemical compound OC(=O)C1=CC=CN=C1NC1=C(F)C=C(C=2C=C(OC(F)(F)F)C=CC=2)C=C1F ZJVWBRDJQSEWGP-UHFFFAOYSA-N 0.000 claims description 2
• UKCUYRNWCBRVBH-UHFFFAOYSA-N 2-[2-chloro-4-[3-(trifluoromethoxy)phenyl]anilino]pyridine-3-carboxylic acid Chemical compound OC(=O)C1=CC=CN=C1NC1=CC=C(C=2C=C(OC(F)(F)F)C=CC=2)C=C1Cl UKCUYRNWCBRVBH-UHFFFAOYSA-N 0.000 claims description 2
• CHZAYPJKCNYCLQ-UHFFFAOYSA-N 2-[4-(2-chlorophenyl)-2,6-difluoroanilino]pyridine-3-carboxylic acid Chemical compound OC(=O)C1=CC=CN=C1NC1=C(F)C=C(C=2C(=CC=CC=2)Cl)C=C1F CHZAYPJKCNYCLQ-UHFFFAOYSA-N 0.000 claims description 2
• ADUJLGYSXJXSKA-UHFFFAOYSA-N 2-[4-(3-ethoxyphenyl)-2-fluoro-5-methylanilino]pyridine-3-carboxylic acid Chemical compound CCOC1=CC=CC(C=2C(=CC(NC=3C(=CC=CN=3)C(O)=O)=C(F)C=2)C)=C1 ADUJLGYSXJXSKA-UHFFFAOYSA-N 0.000 claims description 2
• NAWXUBYGYWOOIX-UHFFFAOYSA-N 2-[[4-[2-(2,4-diaminoquinazolin-6-yl)ethyl]benzoyl]amino]-4-methylidenepentanedioic acid Chemical compound C1=CC2=NC(N)=NC(N)=C2C=C1CCC1=CC=C(C(=O)NC(CC(=C)C(O)=O)C(O)=O)C=C1 NAWXUBYGYWOOIX-UHFFFAOYSA-N 0.000 claims description 2
• RCKCJJYMEDONNF-UHFFFAOYSA-N 3-[4-(3-cyclopropyloxyphenyl)-2-fluoroanilino]pyridine-4-carboxylic acid Chemical compound OC(=O)C1=CC=NC=C1NC1=CC=C(C=2C=C(OC3CC3)C=CC=2)C=C1F RCKCJJYMEDONNF-UHFFFAOYSA-N 0.000 claims description 2
• TVZGACDUOSZQKY-LBPRGKRZSA-N 4-aminofolic acid Chemical compound C1=NC2=NC(N)=NC(N)=C2N=C1CNC1=CC=C(C(=O)N[C@@H](CCC(O)=O)C(O)=O)C=C1 TVZGACDUOSZQKY-LBPRGKRZSA-N 0.000 claims description 2
• ACADWPUQUQUONW-UHFFFAOYSA-N 5-bromo-2-[2-fluoro-4-(3-methoxyphenyl)anilino]pyridine-3-carboxylic acid Chemical compound COC1=CC=CC(C=2C=C(F)C(NC=3C(=CC(Br)=CN=3)C(O)=O)=CC=2)=C1 ACADWPUQUQUONW-UHFFFAOYSA-N 0.000 claims description 2
• SDPBFKBYZUOGDA-UHFFFAOYSA-N 5-chloro-2-(2,6-difluoro-4-phenylanilino)pyridine-3-carboxylic acid Chemical compound OC(=O)C1=CC(Cl)=CN=C1NC1=C(F)C=C(C=2C=CC=CC=2)C=C1F SDPBFKBYZUOGDA-UHFFFAOYSA-N 0.000 claims description 2
• BPIOAXGXBHKHEZ-UHFFFAOYSA-N C1(CC1)C=1C=NC(=C(C(=O)O)C1)NC1=CC(=C(C=C1F)C1=CC(=CC=C1)OC)C.FC=1C(=CC(=C(C1)C1=CC(=CC=C1)OC)C)NC1=C(C(=O)O)C=C(C=N1)C Chemical compound C1(CC1)C=1C=NC(=C(C(=O)O)C1)NC1=CC(=C(C=C1F)C1=CC(=CC=C1)OC)C.FC=1C(=CC(=C(C1)C1=CC(=CC=C1)OC)C)NC1=C(C(=O)O)C=C(C=N1)C BPIOAXGXBHKHEZ-UHFFFAOYSA-N 0.000 claims description 2
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• PCLITLDOTJTVDJ-UHFFFAOYSA-N Chlormethiazole Chemical compound CC=1N=CSC=1CCCl PCLITLDOTJTVDJ-UHFFFAOYSA-N 0.000 claims description 2
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• 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 claims description 2
• 229910052736 halogen Inorganic materials 0.000 claims 2
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